01 — IDENTITY
Is it what we ordered?
Each raw material is identity-tested — usually by HPLC or FTIR — to confirm the compound on the label matches the compound in the drum. Substituted, adulterated, or mislabeled lots get rejected at intake.
From the label to the lab report.
The supplement industry runs on trust the consumer has no way to verify. AgeleX is built the opposite way: every input is identified by brand name, every batch is tested by a third party, and every result can be requested by anyone who buys a bottle. No proprietary blends. No fillers. No assumptions.
How to request your batch report →Trace any bottle to its lab report.
Every bottle of AgeleX is fully traceable. Email support@agelex.us with the lot number printed on the base of your bottle, and we'll send you the Certificate of Analysis for that exact production run — identity, potency, heavy metals, microbial limits — straight from the third-party lab that tested it.
Request a COA
Patented, identified, dosed at the level the research used.
Our NR is nicotinamide riboside — the NAD+ precursor used in the majority of published human research. Our resveratrol is 98% pure trans-isomer, sourced from Japanese knotweed. Our Lion's Mane is a full-spectrum fruiting body extract, not mycelium-on-grain. Brand names appear on the label so they appear in the bottle.
No proprietary blends. Every ingredient on the label shows exactly how many milligrams you're getting. If the dose isn't enough to produce the effect studied in the research, it's not on the label.
Made in the U.S.A. under cGMP audit.
AgeleX is blended, encapsulated, and bottled at a U.S. facility registered with the FDA and audited annually against Current Good Manufacturing Practices. Every batch is traceable from raw material through encapsulation. Every lot gets a unique number printed on the bottle base.
The chain of custody — raw material lot, blending lot, encapsulation lot, bottle lot — is documented for every capsule. We keep those records for the life of the batch and the lifetime of the customer who bought it.
19+
Tests run on every production lot
100%
Of batches tested by an ISO 17025-accredited third-party lab
0
Proprietary blends. Every dose is on the label.
U.S.
Manufactured in an FDA-registered, cGMP-audited facility
How every batch gets verified before it ships.
02 — POTENCY
Is the dose actually in there?
After blending and encapsulation, each batch is assayed for active ingredient concentration. If a capsule claims 500 mg of NR, the assay must show 500 mg ± analytical tolerance, or the lot doesn't ship.
03 — PURITY
Is anything else in there that shouldn't be?
Every lot is screened for the four heavy metals the FDA cares about (lead, arsenic, cadmium, mercury), residual solvents from extraction, and microbial contamination (total plate count, yeast, mold, E. coli, Salmonella).
04 — STABILITY
Will it still be that way at shelf life?
Representative samples from each lot are placed on accelerated and real-time stability programs to confirm potency holds through the printed expiration date — not just on day one.
The standards behind every capsule.
FDA
Registered U.S. manufacturing facility
cGMP
Annual Current Good Manufacturing Practices audit
ISO 17025
Third-party accredited testing on every production lot
NR
Patented NR used in 95%+ of published human NAD+ research
Built to be questioned.
Read the formula, the dosages, and the lab report behind every bottle.
View ingredients Shop AgeleX